Aleksandr A. Sergeev

Two-dimensional lead halide perovskites are of significant interest for a variety of practical applications. However, the relationships between their composition and properties are not fully clear. Here we investigated photoluminescence from 2D Ruddlesden–Popper perovskites with different bulky spacer cations. Significant differences in their optical properties and stability are observed, and perovskites with benzylammonium (BZA) and phenethylammonium (PEA) were selected for more detailed investigation of the observed stability differences due to their similar structure. We find that PEA₂PbI₄ exhibits more narrow emission and increased stability compared to BZA₂PbI₄. In addition, PEA₂PbI₄ exhibits self-healing of defects evident from PL enhancement, which is absent for BZA₂PbI₄. The observed differences between perovskites with BZA and PEA spacer cations can be attributed to differences in the formation of spacer cation vacancies.

Two-dimensional tin halide perovskites are of significant interest for light emitting applications. Here, we investigate the effect of organic cation A on the stability of different Dion–Jacobson tin-based halide perovskites. The ASnBr₄ materials using diammonium cation A with shorter alkyl chains are found to exhibit improved stability, exhibiting dramatic stability difference between the most stable HDASnBr₄, where HDA denotes 1,6-hexanediammonium, and two materials with 8- and 10-carbon alkyl chain ammonium cations. The HDASnBr₄ powders were thermally stable at 100 °C in an argon environment but exhibited decreasing photoluminescence with time in ambient air at 100 °C. The sample degradation at 100 °C is accelerated compared to room temperature, but it proceeds along similar pathways, namely phase transformation followed by perovskite decomposition. Light emission from HDASnBr₄ thin films could be further enhanced by methanol vapor treatment, and warm white emission with Commission Internationale de l’Eclairage (CIE) coordinates (0.37, 0.34) could be obtained by combining HDASnBr₄ with a blue-emitting polymer film, while direct mixing of blue phosphor and HDASnBr₄ powder yields white emission with CIE coordinates of (0.34, 0.32).

Carbon dots can be used for the fabrication of colloidal multi-purpose complexes for sensing and bio-visualization due to their easy and scalable synthesis, control of their spectral responses over a wide spectral range, and possibility of surface functionalization to meet the application task. Here, we developed a chemical protocol of colloidal complex formation via covalent bonding between carbon dots and plasmonic metal nanoparticles in order to influence and improve their fluorescence. We demonstrate how interactions between carbon dots and metal nanoparticles in the formed complexes, and thus their optical responses, depend on the type of bonds between particles, the architecture of the complexes, and the degree of overlapping of absorption and emission of carbon dots with the plasmon resonance of metals. For the most optimized architecture, emission enhancement reaching up to 5.4- and 4.9-fold for complexes with silver and gold nanoparticles has been achieved, respectively. Our study expands the toolkit of functional materials based on carbon dots for applications in photonics and biomedicine to photonics.